CAS 2026-48-4: 1-Butanol, 2-amino-3-methyl-, (2S)-
Formula:C5H13NO
InChI:InChI=1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m1/s1
InChI key:InChIKey=NWYYWIJOWOLJNR-RXMQYKEDSA-N
SMILES:[C@H](C(C)C)(CO)N
Synonyms:- (+)-(S)-Valinol
- (+)-2-Amino-3-methyl-1-butanol
- (+)-Valinol
- (2S)-1-Hydroxy-3-methylbutan-2-amine
- (2S)-2-Amino-3-methyl-1-butanol
- (2S)-Valinol
- (S)-(+)-2-Amino-3-methyl-1-butanol
- (S)-2-Amino-3-methylbutanol
- 1-Butanol, 2-amino-3-methyl-, (S)-
- 1-Butanol, 2-amino-3-methyl-, <span class="text-smallcaps">L</span>-
- 1-Butanol, 2-amino-3-methyl-, L-
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Found 11 products.
(S)-(+)-2-Amino-3-methyl-1-butanol, 96%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C5H13NOPurity:96%Color and Shape:Liquid after melting or solid, Clear colorless to white to light yellowMolecular weight:103.17L-Valinol
CAS:M03447 - L-ValinolFormula:C5H13NOPurity:95%Color and Shape:LiquidMolecular weight:103.16500091552734L-Valinol
CAS:Controlled ProductApplications L-Valinol is used as a reagent in the synthesis of simple 1,3-thiazolidine-2-thione derivatives which can exhibit fungicidal activity. L-Valinol is also used as a reagent in the synthesis of small-molecule inhibitors of MDM2-p53 protein-protein interaction (MDM2 inhibitors) in clinical trials for the treatment of cancer. References Chen, N., et al.: Phosphorus Sulfur, 190, 112 (2015); Zhao, Y., et al.: J. Med. Chem., 58, 1038 (2015)Formula:C5H13NOColor and Shape:WhiteMolecular weight:103.163L-(+)-Valinol, 97%
CAS:L-(+)-Valinol reacts with aldehydes and nitriles to form imines and oxazolines, respectively, for asymmetric synthesis. It is also used for preparation of 4-isopropyloxazolidinones, employed in stereocontrolled aldol and alkylation reactions, synthesis of chiral 2-thiazolidinethiones for aldol reactions, asymmetric alkylation of condensation product with keto acids, asymmetric reactions of its amidines and imines and oxidation of N-protected derivative to the aldehyde. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C5H13NOPurity:97%Color and Shape:Colourless/white to yellow, liquid/low melting solidMolecular weight:103.17L-Valinol
CAS:Formula:C5H13NOPurity:>97.0%(GC)(T)Color and Shape:White or Colorless to Light orange to Yellow powder to lump to clear liquidMolecular weight:103.17(S)-(+)-2-Amino-3-methyl-1-butanol
CAS:(S)-(+)-2-Amino-3-methyl-1-butanolFormula:C5H13NOPurity:97%Color and Shape: colourless to light yellow crystalline solidMolecular weight:103.16g/molL-Valinol
CAS:L-Valinol is a model system that is used to study the reaction of aziridines with oxygen nucleophiles. It has been shown that this reaction proceeds through the formation of an intermediate, hydrogen tartrate, followed by a second step with nitrogen atoms as the nucleophile and alcohol residue as the substrate. The use of L-valinol in asymmetric synthesis was also demonstrated. In this process, amides were obtained with high enantioselectivity by reacting L-valinol with amines in acidic conditions. This synthetic pathway was found to be synergic with other reactions, such as nitroolefination and benzoylation.Formula:C5H13NOPurity:Min. 95%Color and Shape:Solidified MassMolecular weight:103.16 g/molL-Valinol
CAS:Formula:C5H13NOPurity:≥ 97.0%Color and Shape:Colourless to white or pale yellow solid, crystals or liquidMolecular weight:103.17
